Endogenous retroviruses synthesize heterologous chimeric RNAs to reinforce human early embryo development (MLT2A1 ChIRP in 8CLC)
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https://www.ncbi.nlm.nih.gov/sra/SRP507975
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Previous data showed that MLT2A1 RNAs participated in the regulation of totipotent embryo development and totipotent gene expression. Thus, to further study the mechanisms of how MLT2A1 RNAs regulated gene expression, we performed ChIRP-seq to identify the genomic binding sites of MLT2A1 RNAs Overall design: MLT2A1 ChIRP probes were used to precipitate MLT2A1 RNAs and genomic DNA was extracted and sequenced to identify the binding sites of MLT2A1 RNAs by peak calling comparing with input
创建时间：
2026-01-26
